AI Article Synopsis

  • Asparaginase is key in treating pediatric acute lymphoblastic leukemia (ALL) and lymphoblastic lymphoma (LLy), but hypersensitivity to the PEGylated version, pegaspargase, is a common issue.
  • Due to a shortage of the alternative erwinia asparaginase, researchers explored the use of a rapid desensitization protocol to allow safe administration of pegaspargase to patients with a history of hypersensitivity.
  • In a study with ten patients, eight achieved therapeutic levels of asparaginase, and five received multiple doses of pegaspargase without serious reactions, demonstrating the effectiveness of the desensitization approach.

Article Abstract

Asparaginase is an important component of multi-agent chemotherapy for the treatment of pediatric acute lymphoblastic leukemia (ALL) and lymphoblastic lymphoma (LLy). Hypersensitivity to the PEGylated form, pegaspargase, is the most common toxicity observed and is ideally addressed by substituting multiple doses of erwinia asparaginase for each subsequent dose of pegaspargase. An international shortage of erwinia asparaginase has limited the therapeutic options for those experiencing pegaspargase hypersensitivity. Here, we report pegaspargase can be safely administered, while maintaining sustained levels of asparaginase activity, to patients who have had a prior hypersensitivity reaction to pegaspargase by using a standard rapid desensitization protocol. Ten patients with prior hypersensitivity reactions to pegaspargase were treated by using a standardized rapid desensitization protocol. Eight patients had therapeutic asparaginase levels between days 4 and 7 of ≥0.05 IU/mL, and seven patients continued to have sustained levels above ≥0.1 IU/mL between days 10 and 14. Based on chemotherapy regimens, five of these patients successfully received more than one dose of pegaspargase utilizing this protocol.

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Source
http://dx.doi.org/10.1080/08880018.2019.1634778DOI Listing

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